Differential interaction patterns of opioid analgesics with μ opioid receptors correlate with ligand-specific voltage sensitivity

被引:6
|
作者
Kirchhofer, Sina B. [1 ,2 ,3 ,4 ]
Lim, Victor Jun Yu [5 ]
Ernst, Sebastian [1 ]
Karsai, Noemi [2 ,3 ,4 ]
Ruland, Julia G. [1 ]
Canals, Meritxell [2 ,3 ,4 ]
Kolb, Peter [1 ,5 ]
Buenemann, Moritz [1 ]
机构
[1] Univ Marburg, Dept Pharmacol & Clin Pharm, Marburg, Germany
[2] Univ Nottingham, Queens Med Ctr, Sch Life Sci, Div Physiol Pharmacol & Neurosci, Nottingham, England
[3] Univ Birmingham, Ctr Membrane Prot & Receptors, Birmingham, Midlands, England
[4] Univ Nottingham, Ctr Membrane Prot & Receptors, Nottingham, Midlands, England
[5] Univ Marburg, Dept Pharmaceut Chem, Marburg, Germany
来源
ELIFE | 2023年 / 12卷
基金
欧盟地平线“2020”;
关键词
voltage; GPCR; ligands; opioid; Forster resonance energy transfer; binding mode; Human; BINDING; ACTIVATION; DEPENDENCE; EFFICACY; SITE; RECOGNITION; INSIGHTS; MORPHINE;
D O I
10.7554/eLife.91291
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mu opioid receptor (MOR) is the key target for analgesia, but the application of opioids is accompanied by several issues. There is a wide range of opioid analgesics, differing in their chemical structure and their properties of receptor activation and subsequent effects. A better understanding of ligand-receptor interactions and the resulting effects is important. Here, we calculated the respective binding poses for several opioids and analyzed interaction fingerprints between ligand and receptor. We further corroborated the interactions experimentally by cellular assays. As MOR was observed to display ligand-induced modulation of activity due to changes in membrane potential, we further analyzed the effects of voltage sensitivity on this receptor. Combining in silico and in vitro approaches, we defined discriminating interaction patterns responsible for ligand-specific voltage sensitivity and present new insights into their specific effects on activation of the MOR.
引用
收藏
页数:23
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